Philips Issues Correction for Trilogy Evo Ventilators Following FDA Class I Recall
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
Smiths Medical has issued an urgent notification for certain Bivona Tracheostomy Tubes due to a defect that may cause improper ventilation.
Philipsā ventilator recall woes, which stemmed from the machines causing patient health issues, are under investigation by French prosecutors.
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.